Canonical Allele Identifier: CA1328965656

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893253G= , CM000664.2:g.218893253G=	GRCh38
NC_000002.11:g.219757975G= , CM000664.1:g.219757975G=	GRCh37
NC_000002.10:g.219466219G=	NCBI36
NG_012179.1:g.17721G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1236G= MANE Select	ENSP00000258411.3:p.Trp412=
ENST00000258411.7:c.1236G=	ENSP00000258411.3:p.Trp412=
ENST00000489887.1:n.33G=
NM_025216.2:c.1236G=	NP_079492.2:p.Trp412=
XM_011511928.1:c.1185G=	XP_011510230.1:p.Trp395=
XM_011511929.1:c.1140G=	XP_011510231.1:p.Trp380=
XM_011511930.1:c.856G=	XP_011510232.1:p.Gly286=
XM_011511929.2:c.1140G=	XP_011510231.1:p.Trp380=
NM_025216.3:c.1236G= MANE Select	NP_079492.2:p.Trp412=